A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18214569



Internal ID20781610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:120473322..120563752hg38UCSC Ensembl
chr6:120794468..120884898hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3890431
hg1990431
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613144
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18214569
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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